Canonical Allele Identifier: CA324675182

Gene: CYP2D6

Linked Data

• dbSNP Id: rs1555891383

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42130569_42130571del , CM000684.2:g.42130569_42130571del	GRCh38
NG_008376.3:g.4422_4424del
NG_008376.4:g.5241_5243del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.180+42_180+44del	ENSP00000353241.6:n.180+42_180+44del
ENST00000645361.2:c.180+42_180+44del MANE Select	ENSP00000496150.1:n.180+42_180+44del
ENST00000359033.4:c.180+42_180+44del	ENSP00000351927.4:n.180+42_180+44del
ENST00000360608.9:c.180+42_180+44del	ENSP00000353820.5:n.180+42_180+44del
ENST00000389970.7:c.114+42_114+44del	ENSP00000374620.4:n.114+42_114+44del
ENST00000488442.1:n.244_246del
NM_000106.5:c.180+42_180+44del	NP_000097.3:n.180+42_180+44del
NM_001025161.2:c.180+42_180+44del	NP_001020332.2:n.180+42_180+44del
XM_011529966.1:c.180+42_180+44del	XP_011528268.1:n.180+42_180+44del
XM_011529967.1:c.180+42_180+44del	XP_011528269.1:n.180+42_180+44del
XM_011529968.1:c.180+42_180+44del	XP_011528270.1:n.180+42_180+44del
XM_011529969.1:c.38-661_38-659del	XP_011528271.1:n.38-661_38-659del
XM_011529970.1:c.180+42_180+44del	XP_011528272.1:n.180+42_180+44del
XM_011529971.1:c.38-661_38-659del	XP_011528273.1:n.38-661_38-659del
XM_011529972.1:c.180+42_180+44del	XP_011528274.1:n.180+42_180+44del
XR_430455.2:n.209_211del
NM_000106.6:c.180+42_180+44del MANE Select	NP_000097.3:n.180+42_180+44del
XR_002958749.1:n.156_158del
NM_001025161.3:c.180+42_180+44del	NP_001020332.2:n.180+42_180+44del